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CO2018012941A2 - Polymorphic forms of 3- [2-butyl-1- (2-diethylamino-ethyl-1h-benzoimidazol-5-yl] -n-hydroxy-acrylamide and their uses - Google Patents

Polymorphic forms of 3- [2-butyl-1- (2-diethylamino-ethyl-1h-benzoimidazol-5-yl] -n-hydroxy-acrylamide and their uses

Info

Publication number
CO2018012941A2
CO2018012941A2 CONC2018/0012941A CO2018012941A CO2018012941A2 CO 2018012941 A2 CO2018012941 A2 CO 2018012941A2 CO 2018012941 A CO2018012941 A CO 2018012941A CO 2018012941 A2 CO2018012941 A2 CO 2018012941A2
Authority
CO
Colombia
Prior art keywords
benzoimidazol
diethylamino
acrylamide
hydroxy
butyl
Prior art date
Application number
CONC2018/0012941A
Other languages
Spanish (es)
Inventor
David Duncan
Original Assignee
Mei Pharma Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mei Pharma Inc filed Critical Mei Pharma Inc
Publication of CO2018012941A2 publication Critical patent/CO2018012941A2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/14Radicals substituted by nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/08Radicals containing only hydrogen and carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Se describen Polimorfos de Formas cristalinas del 3-[2-butil-1-(2-dietilamino-etil)-1H-benzoimidazol-5-il]-N-hidroxi-acrilamida. También se presentan composiciones farmacéuticas y los usos de las mismas, Formas compuestas y composiciones, para el tratamiento de enfermedades y afecciones.Polymorphs of crystalline forms of 3- [2-butyl-1- (2-diethylamino-ethyl) -1H-benzoimidazol-5-yl] -N-hydroxy-acrylamide are described. Pharmaceutical compositions and their uses, Composite forms and compositions, for the treatment of diseases and conditions are also presented.

CONC2018/0012941A 2016-05-02 2018-11-29 Polymorphic forms of 3- [2-butyl-1- (2-diethylamino-ethyl-1h-benzoimidazol-5-yl] -n-hydroxy-acrylamide and their uses CO2018012941A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662330673P 2016-05-02 2016-05-02
PCT/US2017/030414 WO2017192451A1 (en) 2016-05-02 2017-05-01 Polymorphic forms of 3-[2-butyl-1-(2-diethylamino-ehtyl)-1h-benzoimidazol-5-yl]-n-hydroxy-acrylamide and uses thereof

Publications (1)

Publication Number Publication Date
CO2018012941A2 true CO2018012941A2 (en) 2018-12-28

Family

ID=60203321

Family Applications (1)

Application Number Title Priority Date Filing Date
CONC2018/0012941A CO2018012941A2 (en) 2016-05-02 2018-11-29 Polymorphic forms of 3- [2-butyl-1- (2-diethylamino-ethyl-1h-benzoimidazol-5-yl] -n-hydroxy-acrylamide and their uses

Country Status (20)

Country Link
US (2) US10626092B2 (en)
EP (2) EP3939966A1 (en)
JP (1) JP2019514905A (en)
KR (1) KR20190005904A (en)
CN (1) CN109414425A (en)
AR (1) AR108257A1 (en)
AU (1) AU2017261218A1 (en)
BR (1) BR112018072439A2 (en)
CA (1) CA3022011A1 (en)
CL (1) CL2018003109A1 (en)
CO (1) CO2018012941A2 (en)
EA (1) EA201892341A1 (en)
ES (1) ES2886495T3 (en)
IL (1) IL262578A (en)
MA (1) MA44880A (en)
MX (1) MX382095B (en)
PH (1) PH12018502296B1 (en)
SG (1) SG11201809471UA (en)
TW (1) TW201741286A (en)
WO (1) WO2017192451A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018157742A1 (en) * 2017-02-28 2018-09-07 苏州科睿思制药有限公司 Crystalline form of salt of sb-939, preparation method therefor, and use
WO2019126282A1 (en) 2017-12-19 2019-06-27 Assia Chemical Industries Ltd. Crystalline polymorphs of pracinostat and pracinostat salts
WO2019149262A1 (en) * 2018-02-05 2019-08-08 苏州科睿思制药有限公司 Crystal form of sb-939, preparation method and use thereof
US20230159468A1 (en) 2020-04-22 2023-05-25 Macfarlan Smith Limited Novel forms of pracinostat dihydrochloride

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2291749A1 (en) 1974-11-20 1976-06-18 Delalande Sa 5-carboxyalkyl-benzimidazole derivs - with analgesic, sedative, hypertensive or hypotensive, bronchodilatory, anticholinergic and vasodilatory activity
CA2135173A1 (en) 1992-05-20 1993-11-25 Bruce E. Witzel Ester derivatives of 4-aza-steroids
SE9804212D0 (en) 1998-12-04 1998-12-04 Astra Pharma Prod Compounds
IL144214A0 (en) 1999-01-13 2002-05-23 Warner Lambert Co Benzoheterocycles and their use as mek inhibitors
US6329380B1 (en) 1999-06-30 2001-12-11 Merck & Co., Inc. SRC kinase inhibitor compounds
EP1206265B1 (en) 1999-06-30 2003-11-12 Merck & Co., Inc. Src kinase inhibitor compounds
CN1358094A (en) 1999-07-16 2002-07-10 沃尼尔·朗伯公司 Approaches to treating chronic pain with MEK inhibitors
JP2003504401A (en) 1999-07-16 2003-02-04 ワーナー−ランバート・カンパニー Method for treating chronic pain using MEK inhibitor
GB9919558D0 (en) 1999-08-18 1999-10-20 Hoechst Schering Agrevo Gmbh Fungicidal compounds
US6541661B1 (en) 1999-11-23 2003-04-01 Methylgene, Inc. Inhibitors of histone deacetylase
SK13752001A3 (en) 1999-12-27 2002-07-02 Japan Tobacco, Inc. Fused-ring compounds and use thereof as drugs
US6770666B2 (en) 1999-12-27 2004-08-03 Japan Tobacco Inc. Fused-ring compounds and use thereof as drugs
US6897231B2 (en) 2000-07-31 2005-05-24 Signal Pharmaceuticals, Inc. Indazole derivatives as JNK inhibitors and compositions and methods related thereto
PE20020354A1 (en) 2000-09-01 2002-06-12 Novartis Ag HYDROXAMATE COMPOUNDS AS HISTONE-DESACETILASE (HDA) INHIBITORS
HUP0400651A2 (en) 2000-11-07 2004-06-28 Bristol-Myers Squibb Company Acid derivatives useful as serine protease inhibitors and pharmaceutical compositions containing them
PA8535601A1 (en) 2000-12-21 2002-11-28 Pfizer BENZIMIDAZOL AND PIRIDILIMIDAZOL DERIVATIVES AS LIGANDOS FOR GABAA
WO2003000682A1 (en) 2001-06-25 2003-01-03 Merck & Co., Inc. (pyrimidyl)(phenyl)substituted fused heteroaryl p38 inhibiting and pkg kinase inhibiting compounds
AR035543A1 (en) 2001-06-26 2004-06-16 Japan Tobacco Inc THERAPEUTIC AGENT FOR HEPATITIS C THAT INCLUDES A CONDENSED RING COMPOUND, CONDENSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THAT UNDERSTANDS, BENZIMIDAZOL, THIAZOL AND BIFENYL COMPOUNDS USED AS INTERMEDIARY COMPARTMENTS OF COMPARTMENTS
CA2473505A1 (en) 2002-02-07 2003-08-14 Ellen M. Leahy Novel bicyclic hydroxamates as inhibitors of histone deacetylase
CA2478534A1 (en) 2002-03-13 2003-09-25 Array Biopharma, Inc. N3 alkylated benzimidazole derivatives as mek inhibitors
CA2478374C (en) 2002-03-13 2009-01-06 Eli M. Wallace N3 alkylated benzimidazole derivatives as mek inhibitors
AU2003231359B2 (en) 2002-04-16 2009-04-30 Teijin Limited Piperidine derivatives having CCR3 antagonism
DE10239042A1 (en) 2002-08-21 2004-03-04 Schering Ag New fused macrocyclic pyrimidine derivatives, useful as e.g. cyclin-dependent kinase inhibitors for treating e.g. cancer, autoimmune, cardiovascular or neurodegenerative diseases or viral infections
US7151096B2 (en) 2003-03-05 2006-12-19 Irm Llc Cyclic compounds and compositions as protein kinase inhibitors
CA2518318A1 (en) 2003-03-17 2004-09-30 Takeda San Diego, Inc. Histone deacetylase inhibitors
MY142589A (en) 2003-09-22 2010-12-15 S Bio Pte Ltd Benzimidazole derivatives : preparation and pharmaceutical applications
WO2005066151A2 (en) 2003-12-19 2005-07-21 Takeda San Diego, Inc. Histone deacetylase inhibitors
US20050159470A1 (en) 2003-12-19 2005-07-21 Syrrx, Inc. Histone deacetylase inhibitors
WO2006101456A1 (en) 2005-03-21 2006-09-28 S*Bio Pte Ltd Bicyclic heterocycles hydroxamate compounds useful as histone deacetylase (hdac) inhibitors
CA2540459C (en) * 2005-09-08 2014-02-18 S*Bio Pte Ltd Benzimidazole compounds and uses in treating proliferative disorders
PL1937650T3 (en) * 2005-09-08 2011-11-30 Mei Pharma Inc Heterocyclic compounds
EP2131840B1 (en) 2007-03-07 2018-10-17 MEI Pharma, Inc. Combination of benzimidazole anti-cancer agent and a second anti-cancer agent
EP3662911A1 (en) 2012-10-30 2020-06-10 MEI Pharma, Inc. Combination of azacitidine and pracinostat to treat myelodysplastic syndrome (mds)

Also Published As

Publication number Publication date
US20200317621A1 (en) 2020-10-08
EA201892341A1 (en) 2019-05-31
CN109414425A (en) 2019-03-01
BR112018072439A2 (en) 2019-02-19
EP3452035A1 (en) 2019-03-13
PH12018502296B1 (en) 2022-04-06
ES2886495T3 (en) 2021-12-20
KR20190005904A (en) 2019-01-16
JP2019514905A (en) 2019-06-06
TW201741286A (en) 2017-12-01
AR108257A1 (en) 2018-08-01
WO2017192451A1 (en) 2017-11-09
MX2018013349A (en) 2019-02-20
SG11201809471UA (en) 2018-11-29
PH12018502296A1 (en) 2019-07-08
EP3452035A4 (en) 2019-09-25
EP3939966A1 (en) 2022-01-19
AU2017261218A1 (en) 2018-11-29
IL262578A (en) 2018-12-31
US20190152923A1 (en) 2019-05-23
CA3022011A1 (en) 2017-11-09
MX382095B (en) 2025-03-13
MA44880A (en) 2021-03-17
CL2018003109A1 (en) 2019-04-26
US10626092B2 (en) 2020-04-21
EP3452035B1 (en) 2021-07-07

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